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谁适合接受 CAR-T 细胞治疗?专家对克服转诊障碍的观点

英文原题:Who Is Eligible for Chimeric Antigen Receptor T Cell Therapy? Expert Perspectives on Overcoming Referral Barriers.

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Who Is Eligible for Chimeric Antigen Receptor T Cell Therapy? Expert Perspectives on Overcoming Referral Barriers.

PubMed 2025/10/23(内容时间) Transplant Cell Ther Q1 · IF 4.7(JCR 2025)

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中文摘要

靶向CD19的CAR-T 细胞疗法,包括lisocabtagene maraleucel、axicabtagene ciloleucel和tisagenlecleucel,已改变血液系统恶性肿瘤患者的治疗格局。

然而,识别并转诊可能从治疗中获益的患者仍是一项重大挑战。本文报告了CAR-T 治疗转诊专家建议,这些建议来自10位肿瘤科、血液科、心脏科及感染病学专家在圆桌会议和/或后续审阅中的意见,时间为2024年11月13日至2025年6月9日。专家考量的潜在因素包括年龄、体能状态、疾病状态、心血管功能、肺功能、肾功能、肝功能、感染及心理健康。根据现有证据,专家一致认为,所讨论的任何因素均不应阻止患者接受CAR-T 转诊或进一步评估,尤其考虑到支持治疗的进步以及与其他专科的服务整合。患者的主治肿瘤科医生应在疾病被认定为复发或难治时尽早转诊,最好在开始下一线治疗前,以改善医疗可及性和治疗结局。CAR-T 治疗前,对于肿瘤负荷较高的患者,可在CAR-T 专家会诊后暂停治疗(白细胞单采前)和/或给予桥接治疗(单采后)。根据CAR-T 疗法的安全性特征,专家建议采取灵活的监测方式,并从输注后2周起将患者转回主治或社区肿瘤科医生处继续管理,以提高患者获得这一潜在治愈性治疗的机会。应根据最新法规、政策要求和机构指南,酌情调整临床实践。

总之,10位专家小组建议,对于复发/难治性患者,应及时转诊CAR-T 治疗,并尽量在启动后续治疗线之前完成,以改善医疗可及性和治疗结局。专家指出,只要CAR-T 专家与其他医学专科密切合作,即使患者存在合并症,CAR-T 治疗仍适用于多数患者。美国移植与细胞治疗学会(ASTCT)2025年。由Elsevier公司出版。

展开英文摘要原文

CD19-directed chimeric antigen receptor T-cell (CAR-T) therapies, including lisocabtagene maraleucel, axicabtagene ciloleucel, and tisagenlecleucel, have revolutionized the treatment landscape for patients with hematologic malignancies.

However, identification and referral of patients who could benefit from treatment remains a significant challenge, Here, we report expert recommendations for CAR-T therapy referral gathered from 10 experts in oncology, hematology, cardiology, and infectious diseases from a roundtable meeting and/or subsequent reviews between November 13, 2024, and June 9, 2025.

We considered the following potential factors: age, performance status, disease status, cardiovascular function, pulmonary function, renal function, hepatic function, infections, and psychological health. Based on existing evidence, we agreed that none of the factors discussed should preclude patients from receiving referrals/further evaluation for CAR-T therapy, particularly with current advances in supportive care and integration of services from other specialties. Timely referral should be made by the patient's primary oncologist to specialists as early as the disease is deemed relapsed or refractory, preferably before the starting the subsequent line of therapy to allow better access to care and improve treatment outcomes. Before CAR-T therapy, holding therapy (before leukapheresis) and/or bridging therapy (after leukapheresis) may be given to patients with high-volume disease, in consultation with CAR-T therapy specialists.

Based on the safety profile of CAR-T therapies, experts recommended flexible monitoring and transfer of care back to primary/community oncology physicians, starting from 2 weeks after infusion to improve access to this potentially curative therapy. Adaptations to clinical practice based on the most recent regulations, policy requirements, and institutional guidelines should be made as needed.

In summary, a panel of 10 experts provided recommendations for timely patient referral for CAR-T therapy on the occurrence of relapsed or refractory disease and before the initiation of subsequent lines of therapy to improve care access and treatment outcomes. Experts noted that with close collaboration between CAR-T therapy specialists and other medical disciplines, CAR-T therapy remains a feasible option for most patients despite their comorbidities. 2025 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.

论文信息

作者
Shadman M、Ahmed S、Byrne MT、Chavez JC、Kamdar M、Sorror ML、Perales MA、Hill JA
单位
Department of Cellular Immunotherapy, Fred Hutchinson Cancer Center, University of Washington, Seattle, Washington. Electronic address: mshadman@fredhutch.org.United States
文献类型
综述
期刊
Transplantation and cellular therapy2026 Mar
原文标识
PubMed 41138816 · DOI 10.1016/j.jtct.2025.10.025